Christopher Michael Poteat
Works (4)
Updated: July 5th, 2023 15:29
2021 personal communication
Stereospecific Synthesis of Enantioenriched Alkylidenecyclobutanones via Formal Vinylidene Insertion into Cyclopropanone Equivalents
Poteat, C. M., & Lindsay, V. N. G. (2021, August 20).
TL;DR:
1-Sulfonylcyclopropanols are employed here as efficient cyclopropanone equivalents in a formal vinylidene insertion process, providing the first general synthetic route to enantioenriched alkylidenecyclobutanones after elimination.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, ORCID, NC State University Libraries
Added: August 10, 2021
2020 journal article
Enantioselective Synthesis of Cyclopropanone Equivalents and Application to the Formation of Chiral β-Lactams
Angewandte Chemie International Edition, 59(42), 18655–18661.
author keywords: cycloaddition; lactams; ring expansion; small-ring compounds; synthetic methods
TL;DR:
Both the electronic and steric nature of the sulfonyl moiety were found to have a crucial impact on the rate of equilibration to the corresponding cyclopropanone, highlighting their modular nature and the potential for their widespread adoption as synthetic intermediates.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, ORCID, NC State University Libraries
Added: September 7, 2020
2020 journal article
General Synthesis of Cyclopropanols via Organometallic Addition to 1-Sulfonylcyclopropanols as Cyclopropanone Precursors
Organic Letters, 22(16), 6510–6515.
figshare.com (repository)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, ORCID, NC State University Libraries, Crossref
Added: September 14, 2020
2019 journal article
Controlled -mono- and ,-di-halogenation of alkyl sulfones using reagent-solvent halogen bonding
CHEMICAL COMMUNICATIONS, 55(20), 2912–2915.
TL;DR:
The direct and selective α-mono-bromination of alkyl sulfones was achieved through base-mediated electrophilic halogenation and the mono-halogenation was successfully extended to the fully selective β-chlorination, α-iodination and α-fluorination ofAlkyl sulphones.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, ORCID, NC State University Libraries
Added: April 15, 2019
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